ChemInform Abstract: APPLICATION OF PERICYCLIC REACTIONS TO THE SYNTHESIS OF STRAINED MOLECULES. INTRAMOLECULAR DIELS-ALDER CYCLOADDITIONS. THE SYNTHESIS OF A (Z,Z)-BICYCLO(4.3.1)DECA-1,6-DIENE

1985 ◽  
Vol 16 (31) ◽  
Author(s):  
K. J. SHEA ◽  
L. D. BURKE
ChemInform ◽  
2012 ◽  
Vol 43 (28) ◽  
pp. no-no
Author(s):  
F. Fringuelli ◽  
O. Piermatti ◽  
F. Pizzo ◽  
L. Vaccaro

2019 ◽  
Author(s):  
Evan Darzi ◽  
Joyann Barber ◽  
Neil Garg

We report a modular synthetic strategy for accessing heteroatom-containing polycyclic aromatic hydrocarbons (PAHs) that relies on the controlled generation of transient heterocyclic alkynes and arynes. The strained intermediates undergo in situ trapping with readily accessible oxadiazinones. Four sequential pericyclic reactions occur, namely two Diels–Alder / retro-Diels–Alder sequences, which can be performed in a stepwise or one-pot fashion to assemble four new carbon–carbon (C–C) bonds.


2009 ◽  
Vol 13 (04n05) ◽  
pp. 408-414 ◽  
Author(s):  
Augusto C. Tomé ◽  
Maria G.P.M.S. Neves ◽  
José A.S. Cavaleiro

Porphyrins and other pyrrolic macrocycles can participate in a range of pericyclic reactions. This review deals mainly with their use in Diels-Alder reactions (as dienes and dienophiles) and in 1,3-dipolar cycloadditions (as 1,3-dipoles and dipolarophiles)


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